A Case of Sturge-Weber Syndrome. |
Jun Taek Park1, Geom Hyun Jang1, Jae Kyu Lee1, Kyu Eun Lee1, Jung Hyup Oh2 |
1Department of Pediatrics, Seoul Adventist Hospital, Seoul, Korea 2Department of Ophthalmology, Seoul Adventist Hospital, Seoul,Korea |
Sturge-Weber 증후군의 1례 |
박준택1, 장검현1, 이재규1, 이규은1, 오중협2 |
1서울위생병원 소아과 2서울위생병원 안과 |
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Abstract |
We experienced a case of Sturge-Weber Syndrome in 6 month old male.
The diagnosis was established by charecteristic features of Sturge-Weber Syndrome such as
facial port-wine nevus, focal seizure, hemiparesis, glaucoma and typical calcification & brain
atrophy as on brain CT. Plain radiographys of the skull revealed no evidence of calcification, But the brain C.T.
clearly showed calcific densities. We have presented this case and reviewed the related literature.
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Key Words:
Sturge-Weber Syndrome, Brain CT |
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